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皮质病变程度低与多发性硬化的良性病程有关。

Low degree of cortical pathology is associated with benign course of multiple sclerosis.

机构信息

The Multiple Sclerosis Centre of the Veneto Region, First Neurology Clinic, Department of Neurosciences, University Hospital of Padova, Italy.

出版信息

Mult Scler. 2013 Jun;19(7):904-11. doi: 10.1177/1352458512463767. Epub 2012 Oct 15.

Abstract

BACKGROUND

Although a more favorable course of multiple sclerosis is associated with a low degree of cortical pathology, only longitudinal studies could definitely confirm this association.

MATERIALS AND METHODS

We followed 95 early relapsing-remitting MS (RRMS; median Expanded Disability Status Scale (EDSS) = 1.5, mean disease duration = 3.1 ± 1.3 years) and 45 benign MS patients (EDSS ≤ 3.0, disease duration ≥ 15 years, normal cognition) for 6 years, with EDSS evaluations every 6 months and brain magnetic resonance imaging (MRI) at baseline and then yearly.

RESULTS

At baseline, we detected 406 cortical lesions (CLs) in 67/95 (70.5%) early RRMS and in 24/45 (53.3%) benign MS patients (p = 0.046). After 6 years, the appearance of new CLs was observed in 80/95 (84.2%; 518 CLs) of our early RRMS and in 25/45 (55.5%; 63 CLs; p < 0.001) benign MS patients. At baseline, after corrections for age and disease duration, we observed a cortical thinning of several frontal and temporal regions in our RRMS study patients, compared to the benign MS patients (p ranging between 0.001-0.05). After 6 years, the cortical thinning had increased significantly in several cortices of RRMS patients, but only in the occipital-temporal (p = 0.036) and superior parietal gyrus (p = 0.035) of those with benign MS. Stepwise regression analysis revealed the CL volume (p = 0.006) and the cortical thickness of the temporal middle (p < 0.001), insular long (p < 0.001), superior frontal (p < 0.001) and middle frontal gyri (p < 0.001) as the most sensitive independent predictors of a favorable disease course.

CONCLUSIONS

Our data confirmed that a significantly milder cortical pathology characterizes the most favorable clinical course of MS. Measures of focal and diffuse grey matter should be combined to increase the accuracy in the identification of a benign MS course.

摘要

背景

尽管多发性硬化症(MS)的病程更有利与皮质病变程度较低有关,但只有纵向研究才能明确证实这种关联。

材料与方法

我们对 95 例早期复发缓解型 MS(RRMS;扩展残疾状态量表(EDSS)中位数= 1.5,平均病程= 3.1±1.3 年)和 45 例良性 MS 患者(EDSS≤3.0,病程≥15 年,认知正常)进行了 6 年的随访,每 6 个月进行一次 EDSS 评估,基线和每年进行一次脑部磁共振成像(MRI)检查。

结果

基线时,我们在 67/95(70.5%)例早期 RRMS 和 24/45(53.3%)例良性 MS 患者中发现了 406 个皮质病变(CL)(p=0.046)。6 年后,我们在 80/95(84.2%;518 个 CL)例早期 RRMS 和 25/45(55.5%;63 个 CL)例良性 MS 患者中观察到新的 CL 出现(p<0.001)。基线时,在对年龄和病程进行校正后,我们发现 RRMS 研究患者的几个额颞区皮质变薄,与良性 MS 患者相比(p 介于 0.001-0.05)。6 年后,RRMS 患者的几个皮质变薄明显增加,但只有良性 MS 患者的枕颞部(p=0.036)和顶上回(p=0.035)。逐步回归分析显示 CL 体积(p=0.006)和颞中回皮质厚度(p<0.001)、岛叶长回皮质厚度(p<0.001)、额上回皮质厚度(p<0.001)和额中回皮质厚度(p<0.001)是疾病预后良好的最敏感独立预测因子。

结论

我们的数据证实,皮质病变明显较轻是 MS 最有利临床病程的特征。应结合局灶性和弥漫性灰质测量来提高识别良性 MS 病程的准确性。

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